The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
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As a Clinical Research Associate, you will perform site qualification, initiation, and closeout visits, ensuring regulatory and protocol compliance. Generate queries and manage resolutions with site personnel, documenting activities. Ensure proper recruitment/maintenance plans and act as the primary liaison with site personnel. Manage site's study regulatory documents and assist with audit preparation.
Manage nutritional services at a long-term care facility. You will play a critical role in managing nutritional services at a long-term care facility.